Fotofinder Atbm Master

Fotofinder ATBM Master Recall Summary The Fotofinder ATBM Master device is being recalled in Canada because it is an unauthorized medical device. This device was distributed across Canada. The recall is classified as Class I, which is the most serious type of recall.

Product
Fotofinder ATBM Master
Reason
Unauthorised device
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2025-03-03
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/3b55fa0f-c3eb-42ff-81b3-7f22fd4a2861